FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BEHING-THE-EAR HEARING AID SERIES SP
K Number: K861597
·
Decision Jun 2, 1986
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
58
Review Days
34
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Basic Information
- Device Name
- BEHING-THE-EAR HEARING AID SERIES SP
- K Number
- K861597
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 874.3300
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Applicant
- Maico Hearing Instruments, Inc.
- Date Received
- April 29, 1986
- Decision Date
- June 2, 1986
- Product Code
- ESD
- Advisory Committee
- Ear, Nose, Throat
- Review Advisory Committee
- EN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| ESD | Hearing Aid, Air-Conduction, Prescription | FDA class 1 | Ear, Nose, Throat |
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Other Clearances by Maico Hearing Instruments, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K960031 | AUDIOFLEX 120 | Mar 7, 1996 | Substantially Equivalent |
| K954054 | MAICO PRODIGY CIC SERIES | Sep 28, 1995 | Substantially Equivalent |
| K953161 | MAICO MA630D AUDIOMETER WITH OPTIONAL REFLEX DECAY & EUSTACHIAN TUBE FUNCTION | Jul 24, 1995 | Substantially Equivalent |
| K950637 | MAICO IN-THE-EAR MODEL RD-312 CIC | Mar 21, 1995 | Substantially Equivalent |
| K946253 | MAICO IN-THE-EAR MODEL RD 201 | Jan 30, 1995 | Substantially Equivalent |
| K931322 | KS 5 - CLINICAL AUDIOMETER | Aug 19, 1994 | Substantially Equivalent |
| K933291 | MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AID | Aug 23, 1993 | Substantially Equivalent |
| K930112 | MAICO MA790 AUDIOMETER | Aug 5, 1993 | Substantially Equivalent |
| K926439 | MA25 - PORTABLE AUDIOMETER, MODIFICATION | Aug 5, 1993 | Substantially Equivalent |
| K931160 | SERIES STAR 66 BEKHIND THE EAR HEARING AID | Jun 1, 1993 | Substantially Equivalent |